Research Nurse – Per Diem

Syneos Health

Research Nurse conducting clinical trial visits and coordinating with medical staff for Illingworth Research Group. Ensuring compliance with protocols and maintaining clinical documentation throughout the trial.

Posted 7/2/2026part-timeRemote • Massachusetts • 🇺🇸 United StatesJuniorMid-Level💰 $67,700 - $115,100 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs
Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information
Maintain accurate documentation including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements
Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management and client-facing meetings
Coordinate (working with the RN team) and complete subject trial visits on- and off-site
Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately
Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs
Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents
Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for those patients for on- and off-site care
Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required
Report any suspected misconduct or fraud to Illingworth and associated companies

Requirements

What you’ll need

Registered nurse with a minimum of 2 years' post qualification experience
Research and clinical trials experience with GCP certification
Knowledge of research design and methodology desirable
Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable
Ability to work autonomously with initiative in a team within a multidisciplinary environment
Excellent verbal and written communication skills
Ability to prioritize and manage multiple tasks
Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum

Benefits

Comp & perks

company car or car allowance
Health benefits to include Medical, Dental and Vision
Company match 401k
eligibility to participate in Employee Stock Purchase Plan
Eligibility to earn commissions/bonus based on company and individual performance
flexible paid time off (PTO) and sick time

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Clinical Nursing SkillsTrial Protocol ManagementData DocumentationAdverse Event ReportingPatient Recruitment

Soft Skills

Effective CommunicationTeam CollaborationInitiativeTask Prioritization

Certifications

GCP Certification